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Rust and PyO3 implementation of SCENIC-style regulatory-network analysis. Includes GRN, AUCell, topics, cistarget, peak calling, cell QC, enhancer-gene links, and eRegulon assembly. Installs without dask, Java, or CUDA.

Project description

rustscenic

CI Docs PyPI License: MIT Python Rust Typing

A Rust + PyO3 replacement for the SCENIC / SCENIC+ compute stack: one install, modern Python, low-memory CPU execution, and atlas-scale regulatory-network analysis without Java, dask, CUDA, or fragile multi-tool environments.

pip install rustscenic

Run the full pipeline:

rustscenic pipeline --rna data.h5ad --tfs tfs.txt --output out/

Five runtime dependencies (numpy, pandas, pyarrow, scipy, anndata). Python 3.10 to 3.13, Linux + macOS (x86_64 + aarch64); Windows x64 is covered by the CI and release-wheel workflow for the next release. No dask, no Java, no CUDA.

The practical SCENIC+ compute path in one package:

flowchart LR
    rna["RNA data"] --> network["find gene regulation"]
    network --> regulons["regulons"]
    regulons --> activity["score each cell"]

    motifs["motif data"] --> supported["filter by motif support"]
    regulons --> supported

    atac["ATAC data"] --> topics["discover topics"]
    rna --> enhancers["link enhancers to genes"]
    atac --> enhancers

    supported --> programs["build enhancer-linked regulons"]
    enhancers --> programs

Status

Current release: v0.4.5 on PyPI. This release publishes the MkDocs site, points package metadata at the live docs, declares PEP 561 typing support, and makes CI assert the wheel contains py.typed and _rustscenic.pyi. See CHANGELOG and validation/ for evidence and caveats.

Active limitations are listed under Scope and alternatives, with full detail in site_docs/limitations.md.

Goal

rustscenic is being built as the single-install replacement for the practical SCENIC / SCENIC+ workflow: RNA GRN inference, AUCell regulon activity, motif enrichment, ATAC fragment preprocessing, topic modelling, enhancer-gene linking, and eRegulon assembly in one package.

The project is intentionally not a thin wrapper around the old stack. The target is a simpler architecture that makes regulatory-network analysis easier to install, cheaper to run on CPU, deterministic under a fixed seed, and robust to real atlas conventions such as ENSEMBL var_names, duplicate gene symbols, backed AnnData, and UCSC/Ensembl chromosome mismatches.

What it does

Rust-native replacements for the compute stages plus the glue that scenicplus builds eRegulons from:

Stage rustscenic Replaces
Gene-regulatory network inference rustscenic.grn.infer arboreto.grnboost2
Per-cell regulon activity scoring rustscenic.aucell.score pyscenic.aucell.aucell
Topic modelling on scATAC peaks (Online VB) rustscenic.topics.fit pycisTopic (gensim VB)
Topic modelling K ≥ 30 (Mallet-class collapsed Gibbs) rustscenic.topics.fit_gibbs pycisTopic (Mallet, Java)
Motif-regulon enrichment rustscenic.cistarget.enrich pycistarget AUC kernel
ATAC fragments → cells × peaks matrix rustscenic.preproc.fragments_to_matrix pycisTopic fragment loader
Cell QC (TSS enrichment, FRiP, insert size) rustscenic.preproc.qc pycisTopic.qc
Enhancer → gene correlation rustscenic.enhancer.link_peaks_to_genes scenicplus p2g linking
eRegulon assembly (TF × enhancers × target genes) rustscenic.eregulon.build_eregulons scenicplus eRegulon builder
End-to-end pipeline orchestrator rustscenic.pipeline.run scenicplus snakemake

Bundled with the wheel: HGNC (1,839 human) and MGI (1,721 mouse) TF lists via rustscenic.data.tfs(species). Motif rankings can be fetched and cached via rustscenic.data.download_motif_rankings. Cellxgene-curated h5ads (ENSEMBL IDs in var_names, gene symbols in var["feature_name"]) are auto-detected so atlas data works without manual patching.

Quick example (PBMC-3k, RNA GRN + AUCell)

import anndata as ad
import rustscenic.grn, rustscenic.aucell

import rustscenic.data

adata = ad.read_h5ad("rna.h5ad")
tfs = rustscenic.data.tfs("hs")  # bundled HGNC list (1,839 TFs)

# 1. GRN inference
grn = rustscenic.grn.infer(adata, tf_names=tfs, n_estimators=5000, seed=777)

# 2. Build top-50-target regulons and score per-cell activity
regulons = [
    (f"{tf}_regulon", grn[grn["TF"] == tf].nlargest(50, "importance")["target"].tolist())
    for tf in grn["TF"].unique()
]
auc = rustscenic.aucell.score(adata, regulons, top_frac=0.05)

Full RNA example script: examples/pbmc3k_end_to_end.py. Runs in about 3 minutes on an 8-core laptop with n_estimators=500. docs/tester-quickstart.md is the collaborator smoke-test path.

Focused external-reader docs are in site_docs/ and are built by the docs workflow with MkDocs.

Measured against the pyscenic / arboreto reference

Same input on both sides. Every row has a log file under validation/. For the public benchmark matrix with dataset, command, hardware, baseline, runtime, memory, parity metric and biological sanity check, see site_docs/benchmarks.md.

Axis pyscenic / arboreto rustscenic
Installs on fresh Python 3.10–3.13 venv arboreto: TypeError: Must supply at least one delayed object (dask_expr); pyscenic: ModuleNotFoundError: pkg_resources in current stacks PyPI wheels and sdist install; core APIs import
AUCell wall-time, Ziegler 2021 atlas (31,602 × 59; measured 2026-04 pre-v0.4.x; refresh deferred to v0.5) 6.81 s (pyscenic) 0.25 s
AUCell wall-time, 10x Multiome (10,290 × 1,457; measured 2026-04 pre-v0.4.x; refresh deferred to v0.5) 18.6 s (pyscenic) 0.21 s
Peak RSS, 4 stages on 100,000 cells × 20,292 genes > 40 GB (reported) 6.3 GB
Cistarget kernel vs ctxcore.recovery.aucs reference Pearson 1.0000, mean abs diff 2.4 × 10⁻⁵
AUCell per-cell Pearson vs pyscenic (Ziegler, 31,602 cells; measured 2026-04 pre-v0.4.x; refresh deferred to v0.5) reference 0.984 mean, 91.7 % of cells > 0.95
Canonical airway TFs matching literature (Ziegler, n=14) 8 / 14 (pyscenic, unit weights) 8 / 14 - same hits, same 5/14 misses
Bit-identical output under same seed across threaded runs no (dask non-determinism) yes
Runtime dependencies 40 + 5

Tool-to-tool variation (same hits, same misses on the same 14 canonical TFs) is smaller than the dataset-inherent noise, consistent with rustscenic being numerically equivalent to pyscenic at the per-cell level.

Community validation reports

External collaborator reports complement the maintainer benchmark set. Each row links the public issue or PR plus committed JSON evidence.

Reporter Dataset Stages Result Status
@Skycr Kamath et al. 2022 midbrain dopaminergic neurons, 15,684 cells GRN + cisTarget 266,805 GRN edges, 9 regulons, 9/9 expected DA-neuron TFs recovered issue #68, PR #71, validation/community/kamath_da_grn.json
@lmVl12 10x Multiome GEM-X 10k human brain, immune-subsetted 8,215 cells GRN + AUCell + topics 4,293,902 GRN edges, 1,748 regulons, AUCell/topic outputs non-empty; neural signal improved after immune subsetting issues #69, #70, PR #74, validation/community/human_brain_10k_v0.4.1.json

Per-stage detail

Numbers are rustscenic's values. The measurement context (dataset, n_cells, version) is in each row. The parity refresh against current upstream stacks (six-dataset sweep) is now planned for v0.5+; see docs/v0.4.x-benchmark-plan.md for the dataset list and success criteria.

GRN - arboreto.grnboost2 replacement

Measurement Value
Per-edge Spearman vs arboreto (PBMC-3k scanpy, n_estimators=5000, 480,680 shared edges, v0.3.10) 0.611
Within-TF Spearman, mean across 1,274 TFs (same fixture) 0.632 (median 0.649)
Per-edge Spearman vs arboreto (multiome3k, n_estimators=5000, 816 k common edges, 2026-04) 0.58
Per-target TF-ranking Spearman mean 0.57
TRRUST known TF→target edges recovered (PBMC-3k) 17 / 18 (94 %)
Lineage TFs correctly enriched in expected cell types (PBMC-10k) 8 / 8 (SPI1, PAX5, EBF1, TCF7, LEF1, TBX21, CEBPD, IRF8)
Cortex marker TFs present in regulon set (E18 multiome, 4,770 cells, v0.3.10; name-presence, not cell-type enrichment) 9 / 9 (Pax6, Neurod2, Sox2, Ascl1, Tbr1, Neurog2, Fezf2, Eomes, Foxg1)
MITF regulon activity, Tirosh 2016 melanoma - malignant vs TME 3.48×
Wall vs pyscenic on PBMC-3k (n_estimators=5000, seed 777, Apple M5, v0.3.10; pyscenic in sync mode - not apples-to-apples against dask-parallel) 214 s vs 381 s (1.78×)
100k-cell bootstrap, n_estimators=100 17 min / 5.0 GB peak RSS

At high cell counts, GRN target blocking is adaptive by default. Users can force a specific response-block width with rustscenic.grn.infer(..., target_block_size=32) or rustscenic grn --target-block-size 32 when benchmarking cache/RSS behaviour.

Edge rankings disagree with arboreto at fine grain (per-edge Spearman 0.611 on PBMC-3k v0.3.10 / 0.58 on multiome3k 2026-04, top-10k Jaccard 0.20) - expected consequence of independent histogram-GBM quantisation. Coarse biology converges (per-TF Spearman ≈ 0.65, all canonical lineage TFs recovered on both human PBMC and mouse cortex). Downstream AUCell is 0.99 per-cell with pyscenic, so edge-ranking differences do not propagate.

AUCell - pyscenic.aucell replacement

Measurement Value
Per-cell Pearson vs pyscenic (10x Multiome, 2,588 × 1,457) 0.988 mean, 99.5 % of cells > 0.95
Per-cell Pearson vs pyscenic (Ziegler atlas, 31,602 × 59) 0.984 mean, 91.7 % of cells > 0.95
Per-regulon Pearson (10x Multiome) 0.87 mean, 90.5 % > 0.80
Exact top-regulon-per-cell match (Multiome) 88.4 %
Wall-time, 10k cells × 1,457 regulons 0.21 s (vs 18.6 s pyscenic)
100 k cells × 500 regulons 10 s, 5.6 GB peak RSS

Topics - pycisTopic LDA replacement (Online VB + collapsed Gibbs)

Two algorithms ship side-by-side:

  • rustscenic.topics.fit - Online VB LDA, fastest at K ≤ 10.
  • rustscenic.topics.fit_gibbs - collapsed Gibbs (Mallet's algorithm class). Add n_threads=N for parallel AD-LDA.

Real PBMC 3k Multiome ATAC, 1,500 cells × 98,319 peaks, K = 30, intrinsic top-10 NPMI on the training corpus:

Tool Wall Unique topics (of 30) Top-10 NPMI mean
rustscenic.topics.fit (Online VB) 104 s 2 / 30 (collapsed) +0.012
rustscenic.topics.fit_gibbs (serial) 191 s 22 / 30 +0.031
rustscenic.topics.fit_gibbs (8-thread) 84 s 25 / 30 +0.019
Mallet (pycisTopic reference) n/a 24 / 30 0.196 (extrinsic)

Collapsed Gibbs gives ~11× more distinct topics than Online VB on sparse scATAC at K = 30 and ~2.7× higher intrinsic NPMI; the parallel AD-LDA path adds a 2.56× wall-clock speedup at 8 threads while preserving topic diversity. Mallet's published 0.196 is an extrinsic NPMI (different protocol, not directly comparable in absolute scale). See docs/topic-collapse.md and docs/bench-vs-references.md. Reproduce with python validation/scaling/bench_npmi_head_to_head.py and python validation/scaling/bench_gibbs_parallel.py.

Cistarget - pycistarget AUC kernel replacement

Validated on the aertslab hg38 v10 feather database (5,876 motifs × 27,015 genes):

Measurement Value
Per-regulon Pearson vs ctxcore.recovery.aucs (58 TRRUST regulons) 1.0000 (all > 0.9999, abs diff 2.4 × 10⁻⁵)
Self-consistency (motif's own top-500 genes → rank #1) 10 / 10
TRRUST at scale (166 TFs ≥ 10 targets): TF-annotated motif ranks #1 19 %
Same benchmark: any TF-motif in top-100 68 – 100 % (rises with regulon size)
Mouse mm10 cross-species (5 TRRUST TFs) 2 / 5 rank #1, 4 / 5 in top-5
100 k-cell workload × 100 regulons 2.6 s, 6.3 GB peak RSS

Bit-identical to ctxcore.recovery.aucs at float32 precision. The 19 % rank-#1 rate is the scaled-out TRRUST-vs-motif-binding benchmark, a property of the gold-standard mismatch, not the implementation.

End-to-end + determinism

Pipeline Wall Peak RSS Stages
Reference (arboreto + pyscenic + tomotopy), 10x Multiome 3k 11.8 min n/a 4
rustscenic, 10x Multiome 3k 9.1 min n/a 4
rustscenic, 10x PBMC 3k multiome real-data (v0.3.9, measured 2026-05-02) 7.5 min 3.67 GB 7 (all)
rustscenic, 10x brain E18 5k multiome real-data (v0.3.10, measured 2026-05-04) 13.8 min 4.01 GB 7 (all)
rustscenic, 10x PBMC granulocyte 10k multiome real-data (v0.4.3, measured 2026-05-11) 38.1 min 5.39 GB 7 (all)
rustscenic, 100k synthetic multiome E2E (measured v0.3.10, 2026-04-27) 12.7 min 7.09 GB 7 (all)
rustscenic, 200k synthetic multiome E2E (measured v0.3.10, 2026-04-27) 16.8 min 7.44 GB 7 (all)

Real 10x multiome scaling from 2,767 to 11,620 cells:

  • cell count: 4.2x
  • wall time: 5.1x, slope about 1.21 over the full span
  • peak RSS: 1.47x
  • 10k PBMC granulocyte run recovered 10 of 10 canonical TFs by name
  • brain E18 5k run recovered 9 of 9 cortex TFs by name

Name-presence checks are not cell-type enrichment tests. Synthetic 100k and 200k runs are scale gates, not biological validation. Full commands, hardware, baseline status, and caveats are in site_docs/benchmarks.md.

Scope and alternatives

rustscenic covers the practical SCENIC / SCENIC+ compute path on CPU. Adjacent tools with different scope:

  • GPU, CUDA - flashSCENIC (uses RegDiffusion, a different algorithm from GENIE3 / GRNBoost2, so outputs are not pyscenic-numerical).
  • Multiomic enhancer-aware GRN - scenicplus (joint scRNA + scATAC enhancer inference; superset of this scope).
  • TF-activity scoring from prebuilt regulons, no GRN inference - decoupler-py with CollecTRI.
  • R Bioconductor ecosystem - the original R-SCENIC or Epiregulon.

rustscenic does not bundle the aertslab motif ranking feather databases (300 MB – 35 GB). Users fetch them from resources.aertslab.org and pass the resulting DataFrame to cistarget.enrich.

Current limitations before treating rustscenic as a full SCENIC+ replacement:

  • refreshed AUCell timings against current upstream stacks
  • region-cisTarget parity checks on real region-ranking databases
  • six-dataset benchmark sweep planned for v0.5+
  • cell-type enrichment checks for biology claims, not only TF-name recovery
  • smoother raw 10x pipeline.run input without caller-side ATAC subsetting

Per-stage CLI

rustscenic grn       --expression data.h5ad --tfs tfs.txt --output grn.parquet
rustscenic aucell    --expression data.h5ad --regulons grn.parquet --output auc.parquet
rustscenic topics    --expression atac.h5ad --output topics --n-topics 30
rustscenic cistarget --rankings motifs.feather --regulons grn.parquet --output enrichment.tsv

Repo layout

  • crates/ - Rust workspace: rustscenic-{grn, aucell, topics, preproc, py}
  • python/rustscenic/ - Python package, CLI entry point, type stubs
  • examples/pbmc3k_end_to_end.py - RNA GRN + AUCell script on real PBMC-3k
  • validation/ - reproducible benchmark scripts + measurement reports for every number above, plus VALIDATION_SUMMARY.md
  • tests/ - pytest suite (169 Python tests, 1 skipped) + Rust crate tests (57)
  • manuscript/ - preprint source
  • docs/topic-collapse.md - known algorithmic caveat

License

MIT. Algorithm implementations follow the aertslab Python references - original method credit to Aibar et al. 2017 (SCENIC), Bravo González-Blas et al. 2023 (SCENIC+), Hoffman-Blei-Bach 2010 (Online VB LDA).

Citation and attribution

If you use rustscenic in a paper, report, benchmark, derivative package, or lab workflow, cite the exact release used. GitHub citation metadata is in CITATION.cff.

rustscenic was created and is maintained by Ekin Kahraman. See AUTHORS.md and docs/collaboration-and-authorship.md for contribution and authorship expectations.

Contact

File issues at github.com/Ekin-Kahraman/rustscenic/issues. Bug, correctness, and validation-report templates pre-fill the fields we need. If you ran the pipeline on real data and want the result folded into the v0.4.x sweep, see docs/tester-reporting.md. If reporting ARI or related clustering metrics, include the comparator; see docs/evaluation-metrics.md. Coordinated vulnerability disclosure: see SECURITY.md.

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